119 related articles for article (PubMed ID: 22733243)
1. [Genetic variations of a tumor].
Yazdi AS
Hautarzt; 2012 Jul; 63(7):587-8. PubMed ID: 22733243
[No Abstract] [Full Text] [Related]
2. Common Variants Affecting Susceptibility to Develop Multiple Basal Cell Carcinomas.
Verkouteren JAC; Pardo LM; Uitterlinden AG; Hofman A; Nijsten T
J Invest Dermatol; 2015 Aug; 135(8):2135-2138. PubMed ID: 25801793
[No Abstract] [Full Text] [Related]
3. [Molecular diagnosis of melanocytic tumors].
Bauer J
Hautarzt; 2016 Jan; 67(1):59-63. PubMed ID: 26589514
[TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of desmoid tumors: decryption of the enigma.
Place TL; Mezhir JJ
Onkologie; 2012; 35(11):641-2. PubMed ID: 23147539
[No Abstract] [Full Text] [Related]
5. Rapidly metastasizing malignant melanoma characterized by a rare BRAF mutation not responding to vemurafenib.
Starz H; Gutschi M; Welzel J; Haas C
J Dtsch Dermatol Ges; 2014 Feb; 12(2):151-4. PubMed ID: 24238398
[No Abstract] [Full Text] [Related]
6. Expanding cancer predisposition genes with ultra-rare cancer-exclusive human variations.
Rasnic R; Linial N; Linial M
Sci Rep; 2020 Aug; 10(1):13462. PubMed ID: 32778766
[TBL] [Abstract][Full Text] [Related]
7. Genomics: The search for association.
Baker M
Nature; 2010 Oct; 467(7319):1135-8. PubMed ID: 20981103
[No Abstract] [Full Text] [Related]
8. Natural history of Kindler syndrome and propensity for skin cancer - case report and literature review.
Saleva M; Has C; He Y; Vassileva S; Balabanova M; Miteva L
J Dtsch Dermatol Ges; 2018 Mar; 16(3):338-341. PubMed ID: 29384271
[No Abstract] [Full Text] [Related]
9. Establishment of a Radiogenomics Consortium.
West C; Rosenstein BS; Alsner J; Azria D; Barnett G; Begg A; Bentzen S; Burnet N; Chang-Claude J; Chuang E; Coles C; De Ruyck K; De Ruysscher D; Dunning A; Elliott R; Fachal L; Hall J; Haustermans K; Herskind C; Hoelscher T; Imai T; Iwakawa M; Jones D; Kulich C; ; Langendijk JH; O'Neils P; Ozsahin M; Parliament M; Polanski A; Rosenstein B; Seminara D; Symonds P; Talbot C; Thierens H; Vega A; West C; Yarnold J
Int J Radiat Oncol Biol Phys; 2010 Apr; 76(5):1295-6. PubMed ID: 20338472
[No Abstract] [Full Text] [Related]
10. Common variants of the EPDR1 gene and the risk of Dupuytren’s disease.
Dębniak T; Żyluk A; Puchalski P; Serrano-Fernandez P
Handchir Mikrochir Plast Chir; 2013 Oct; 45(5):253-7. PubMed ID: 24089297
[TBL] [Abstract][Full Text] [Related]
11. Identification of rare, disease-associated variants in the promoter region of the RNF114 psoriasis susceptibility gene.
Onoufriadis A; Simpson MA; Burden AD; Barker JN; Trembath RC; Capon F
J Invest Dermatol; 2012 Apr; 132(4):1297-9. PubMed ID: 22205304
[No Abstract] [Full Text] [Related]
12. Association of IRF4 single-nucleotide polymorphism rs12203592 with melanoma-specific survival.
Ward SV; Gibbs DC; Orlow I; Thomas NE; Kanetsky PA; Luo L; Cust AE; Anton-Culver H; Gruber SB; Gallagher RP; Rosso S; Zanetti R; Dwyer T; Begg CB; Berwick M;
Br J Dermatol; 2020 Jul; 183(1):163-165. PubMed ID: 31958143
[No Abstract] [Full Text] [Related]
13. Genetic Variations in ABCG2 Gene Predict Breast Carcinoma Susceptibility and Clinical Outcomes after Treatment with Anthracycline-Based Chemotherapy.
Wu H; Liu Y; Kang H; Xiao Q; Yao W; Zhao H; Wang E; Wei M
Biomed Res Int; 2015; 2015():279109. PubMed ID: 26634205
[TBL] [Abstract][Full Text] [Related]
14. [From genetic variants to pathophysiology?-Genome-wide association study in malignant melanoma].
Albuscheit N; Yazdi AS
Hautarzt; 2021 Jan; 72(1):88-90. PubMed ID: 33140834
[No Abstract] [Full Text] [Related]
15. Variation on a theme: identifying sequence variation in disease genes and defining pathogenicity.
Clark LN
Neurology; 2009 Jun; 72(22):1882-3. PubMed ID: 19386995
[No Abstract] [Full Text] [Related]
16. Are cubilin (CUBN) variants at the heart of urinary albumin excretion?
O'Toole JF; Sedor JR
J Am Soc Nephrol; 2011 Mar; 22(3):404-6. PubMed ID: 21372212
[No Abstract] [Full Text] [Related]
17. Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population.
Verstraeten A; Wauters E; Crosiers D; Meeus B; Corsmit E; Elinck E; Mattheijssens M; Peeters K; Cras P; Pickut B; Vandenberghe R; Engelborghs S; De Deyn PP; Van Broeckhoven C; Theuns J
Neurobiol Aging; 2012 Aug; 33(8):1844.e11-3. PubMed ID: 22336192
[TBL] [Abstract][Full Text] [Related]
18. Sézary syndrome: old enigmas, new targets.
Nicolay JP; Felcht M; Schledzewski K; Goerdt S; Géraud C
J Dtsch Dermatol Ges; 2016 Mar; 14(3):256-64. PubMed ID: 26972187
[TBL] [Abstract][Full Text] [Related]
19. [Genetic associate studies in multifactorial genetic diseases].
Breuning MH
Ned Tijdschr Geneeskd; 2009 Mar; 153(10):428-9. PubMed ID: 19374090
[No Abstract] [Full Text] [Related]
20. Cysteine-sparing notch3 mutations: cadasil or cadasil variants?
Quattrone A; Mazzei R
Neurology; 2009 Jun; 72(24):2135-6; author reply 2136. PubMed ID: 19528524
[No Abstract] [Full Text] [Related]
[Next] [New Search]